FI970317A - Som antiproliferativa ämnen och Garft-inhibitorer användbara föreningar - Google Patents

Som antiproliferativa ämnen och Garft-inhibitorer användbara föreningar Download PDF

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Publication number
FI970317A
FI970317A FI970317A FI970317A FI970317A FI 970317 A FI970317 A FI 970317A FI 970317 A FI970317 A FI 970317A FI 970317 A FI970317 A FI 970317A FI 970317 A FI970317 A FI 970317A
Authority
FI
Finland
Prior art keywords
compounds
antiproliferative agents
compounds useful
garft inhibitors
garft
Prior art date
Application number
FI970317A
Other languages
English (en)
Finnish (fi)
Other versions
FI970317A0 (sv
FI112079B (sv
Inventor
Michael D Varney
William H Romines
Original Assignee
Agouron Pharma
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Agouron Pharma filed Critical Agouron Pharma
Publication of FI970317A0 publication Critical patent/FI970317A0/sv
Publication of FI970317A publication Critical patent/FI970317A/sv
Application granted granted Critical
Publication of FI112079B publication Critical patent/FI112079B/sv

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/38—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems
FI970317A 1994-07-28 1997-01-24 2-(2-amino-4-okso-tetrahydropyrido[2,3-d]-pyridin- och pyrimido[5,4-b][1,4]tiazin-6-yl)etyl-4-metyltien-2-yl-L-glutaminsyraderivat FI112079B (sv)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US28163994 1994-07-28
US08/281,639 US5608082A (en) 1994-07-28 1994-07-28 Compounds useful as antiproliferative agents and GARFT inhibitors
PCT/US1995/009519 WO1996003406A1 (en) 1994-07-28 1995-07-28 Compounds useful as antiproliferative agents and garft inhibitors
US9509519 1995-07-28

Publications (3)

Publication Number Publication Date
FI970317A0 FI970317A0 (sv) 1997-01-24
FI970317A true FI970317A (sv) 1997-03-05
FI112079B FI112079B (sv) 2003-10-31

Family

ID=23078167

Family Applications (1)

Application Number Title Priority Date Filing Date
FI970317A FI112079B (sv) 1994-07-28 1997-01-24 2-(2-amino-4-okso-tetrahydropyrido[2,3-d]-pyridin- och pyrimido[5,4-b][1,4]tiazin-6-yl)etyl-4-metyltien-2-yl-L-glutaminsyraderivat

Country Status (20)

Country Link
US (2) US5608082A (sv)
EP (1) EP0773943B1 (sv)
JP (1) JPH10503762A (sv)
KR (1) KR100380610B1 (sv)
CN (2) CN1091770C (sv)
AT (1) ATE206122T1 (sv)
AU (1) AU697138B2 (sv)
CA (1) CA2195420A1 (sv)
DE (1) DE69522945T2 (sv)
DK (1) DK0773943T3 (sv)
ES (1) ES2162933T3 (sv)
FI (1) FI112079B (sv)
MX (1) MX9700675A (sv)
NO (1) NO308248B1 (sv)
NZ (1) NZ290703A (sv)
PT (1) PT773943E (sv)
RU (1) RU2152945C2 (sv)
SI (1) SI0773943T1 (sv)
TW (1) TW432062B (sv)
WO (1) WO1996003406A1 (sv)

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US5831100A (en) * 1995-06-07 1998-11-03 Agouron Pharmaceuticals, Inc. Syntheses of optically pure compounds useful as GARFT inhibitors and their intermediates
CA2383524C (en) * 1999-08-31 2010-09-28 Merck & Co., Inc. Thiazolyl alkynyl compounds and methods of use thereof
US6774138B2 (en) 1999-08-31 2004-08-10 Merck & Co., Inc. Thiazolyl(pyridyl)ethyne compounds
WO2002078709A2 (en) * 2001-02-16 2002-10-10 Eli Lilly And Company Use of pyrido`2,3-d pyrimidin derivatives for the treatment of human cytomegalovirus infections
WO2003033478A1 (en) * 2001-10-12 2003-04-24 Warner-Lambert Company Llc Alkynylated fused ring pyrimidine compounds as matrix metalloprotease-13 inhibitors
CA2462442A1 (en) 2001-10-12 2003-04-24 Warner-Lambert Company Llc Alkyne matrix metalloproteinase inhibitors
WO2003033477A1 (en) * 2001-10-12 2003-04-24 Warner-Lambert Company Llc Alkynlated fused ring pyrimidine compounds as matrix metalloprotease-13 inhibitor
US6962922B2 (en) * 2001-10-12 2005-11-08 Warner-Lambert Company Llc Alkynylated quinazoline compounds
US20040043959A1 (en) * 2002-03-04 2004-03-04 Bloom Laura A. Combination therapies for treating methylthioadenosine phosphorylase deficient cells
US6747147B2 (en) 2002-03-08 2004-06-08 Warner-Lambert Company Oxo-azabicyclic compounds
US6894057B2 (en) * 2002-03-08 2005-05-17 Warner-Lambert Company Oxo-azabicyclic compounds
US20040006077A1 (en) * 2002-06-25 2004-01-08 Bernard Gaudilliere Thiazine and oxazine derivatives as MMP-13 inhibitors
CA2489722A1 (en) * 2002-07-17 2004-01-22 William Howard Roark Combination of an allosteric alkyne inhibitor of matrix metalloproteinase-13 with celecoxib or valdecoxib
WO2004113337A1 (en) * 2003-06-25 2004-12-29 Pfizer Inc. Convergent synthesis of a garft inhibitor containing a methyl substitute thiophene core and a tetrahydropyrido`2,3-d! pyrimidine ring system and intermediates therefor
WO2004113328A1 (en) * 2003-06-25 2004-12-29 Pfizer Inc. Convergent asymmetric synthesis route to produce a key intermediate towards the synthesis of a garft inhibitor
WO2005016926A1 (en) * 2003-08-19 2005-02-24 Warner-Lambert Company Llc Pyrido [3,4-d] pyrimidine derivatives as matrix metalloproteinase-13 inhibitors
US7420059B2 (en) * 2003-11-20 2008-09-02 Bristol-Myers Squibb Company HMG-CoA reductase inhibitors and method
AU2006238930B2 (en) 2005-04-26 2010-12-23 Pfizer Inc. P-cadherin antibodies
ES2546069T3 (es) 2005-09-07 2015-09-18 Amgen Fremont Inc. Anticuerpos monoclonales humanos para quinasa-1 de tipo receptor de activina (ALK-1)
EP2021338A1 (en) 2006-05-09 2009-02-11 Pfizer Products Inc. Cycloalkylamino acid derivatives and pharmaceutical compositions thereof
US8252804B2 (en) 2008-10-01 2012-08-28 Duquesne University Of The Holy Spirit Selective proton coupled folate transporter and folate receptor, and GARFTase inhibitor compounds and methods of using the same
LT2678327T (lt) 2011-02-23 2016-11-25 Lupin Limited Heteroarilo dariniai kaip nachr alpha7 moduliatoriai
GB201103578D0 (en) 2011-03-02 2011-04-13 Sabrepharm Ltd Dipyridinium derivatives
ES2606043T3 (es) 2011-07-05 2017-03-17 Lupin Limited Derivados de biarilo como moduladores de nAChR
EP2760820A4 (en) * 2011-09-29 2015-04-29 Univ Emory SPHINGOSIN ANALOGS, COMPOSITIONS AND METHODS RELATED THERETO
CA2866015A1 (en) 2012-03-06 2013-09-12 Lupin Limited Thiazole derivatives as alpha 7 nachr modulators
GB2543550A (en) 2015-10-21 2017-04-26 Hox Therapeutics Ltd Peptides
CN115634228B (zh) * 2021-07-20 2024-03-19 首都医科大学 嘌呤合成抑制剂在制备治疗缺血和缺血再灌注损伤药物中的应用

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AT376436B (de) * 1982-11-05 1984-11-26 Laevosan Gmbh & Co Kg Verfahren zur herstellung neuer thiophen-2carbons[urederivate und pharmazeutisch vertraeglicher saeure- oder basenadditionssalze davon
US4927828A (en) * 1985-03-08 1990-05-22 The Trustees Of Princeton University Diastereoisomeric tetrahydropyrido-(2,3,d) pyrimidine derivatives
US4684653A (en) * 1985-03-08 1987-08-04 The Trustees Of Princeton University Pyrido(2,3-d)pyrimidine derivatives
US5026851A (en) * 1985-03-08 1991-06-25 The Trustees Of Princeton University Pyrido[2,3-]pyrimidine derivatives
US4831037A (en) * 1987-04-20 1989-05-16 The Trustees Of Princeton University 4 (3H)-oxo-5,6,7,8-tetrahydropyrido-(2,3-d)pyrimidine derivatives
US4988813A (en) * 1986-10-20 1991-01-29 The Trustees Of Princeton University Process for the preparation of fused pyridine compounds
US4895946A (en) * 1987-10-26 1990-01-23 The Trustees Of Princeton University Process for the preparation of fused pyridine compounds
US4889859A (en) * 1988-02-05 1989-12-26 The Trustees Of Princeton University Pyrido[2,3-d]pyrimidine derivatives
US4882334A (en) * 1988-05-25 1989-11-21 The Trustees Of Princeton University N-(5,6,7,8-tetrahydropyrido]2,3-d]pyrimidin-6-ylethl-thineyl-and furylcarbonyl)-glutamic acid derivatives
DK172753B1 (da) * 1988-05-25 1999-06-28 Lilly Co Eli N-(5,6,7,8-tetrahydropyrido[2,3--d]pyrimidin-6-yl-alkanoyl)-glutaminsyrederivater, deres anvendelse, farmaceutiske præparat
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US4871746A (en) * 1988-05-31 1989-10-03 The Trustees Of Princeton University N-[N-(tetrahydropyrido[2,3-D]pyrimidinylmethyl)-aminomethylbenzoyl]glutamic acid derivatives as neoplastic growth inhibitors
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EP0438261A3 (en) * 1990-01-16 1992-02-26 Takeda Chemical Industries, Ltd. Condensed heterocyclic glutamic acid derivatives, their production and use
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Also Published As

Publication number Publication date
MX9700675A (es) 1997-04-30
NO970349L (no) 1997-03-12
CA2195420A1 (en) 1996-02-08
ATE206122T1 (de) 2001-10-15
AU3151795A (en) 1996-02-22
CN1091770C (zh) 2002-10-02
JPH10503762A (ja) 1998-04-07
US5646141A (en) 1997-07-08
RU2152945C2 (ru) 2000-07-20
ES2162933T3 (es) 2002-01-16
NO308248B1 (no) 2000-08-21
TW432062B (en) 2001-05-01
FI970317A0 (sv) 1997-01-24
FI112079B (sv) 2003-10-31
KR100380610B1 (ko) 2003-08-27
PT773943E (pt) 2002-01-30
EP0773943B1 (en) 2001-09-26
AU697138B2 (en) 1998-09-24
CN1394857A (zh) 2003-02-05
DK0773943T3 (da) 2002-03-04
SI0773943T1 (en) 2001-12-31
US5608082A (en) 1997-03-04
NZ290703A (en) 1998-11-25
CN1154110A (zh) 1997-07-09
DE69522945T2 (de) 2002-03-28
EP0773943A1 (en) 1997-05-21
WO1996003406A1 (en) 1996-02-08
NO970349D0 (no) 1997-01-27
DE69522945D1 (de) 2001-10-31

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